A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526188



Internal ID22395568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:2776262..2890633hg38UCSC Ensembl
chrX:2694303..2808674hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38114372
hg19114372
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14350951, nssv14350949, nssv14350948, nssv14350950, nssv14350947
SamplesNA19238, NA19239, HG00732, NA19240, HG00733
Known GenesGYG2, XG
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526188
Frequency
Sample Size9
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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